journal article·2013-12-23

Direct Observation and Control of Supported Lipid Bilayer Formation with Interferometric Scattering Microscopy

Joanna Andrecka, Katelyn M. Spillane, Jaime Ortega-Arroyo, Philipp Kukura

ACS Nano· Volume 7· Issue 12
Publisher page

Abstract

Supported lipid bilayers (SLB) are frequently used to study processes associated with or mediated by lipid membranes. The mechanism by which SLBs form is a matter of debate, largely due to the experimental difficulty associated with observing the adsorption and rupture of individual vesicles. Here, we used interferometric scattering microscopy (iSCAT) to directly visualize membrane formation from nanoscopic vesicles in real time. We observed a number of previously proposed phenomena such as vesicle adsorption, rupture, movement, and a wave-like bilayer spreading. By varying the vesicle size and the lipid-surface interaction strength, we rationalized and tuned the relative contributions of these phenomena to bilayer formation. Our results support a model where the interplay between bilayer edge tension and the overall interaction energy with the surface determine the mechanism of SLB formation. The unique combination of sensitivity, speed, and label-free imaging capability of iSCAT provides exciting prospects not only for investigations of SLB formation, but also for studies of assembly and disassembly processes on the nanoscale with previously unattainable accuracy and sensitivity.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Lipid Membrane Structure and Behavior · Advanced Fluorescence Microscopy Techniques · Glycosylation and Glycoproteins Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Physical and Theoretical Chemistry Laboratory, Department of Chemistry, University of Oxford, South Parks Road, Oxford OX1 3QZ, United Kingdom.

References (50)

Show source-provided references
1. Sackmann E. · Science · 1996 · 271 · 4310.1126/science.271.5245.43 ↗
2. Brian A. A. · Proc. Natl. Acad. Sci. U.S.A. · 1984 · 81 · 615910.1073/pnas.81.19.6159 ↗
3. Hartman N. C. · Proc. Natl. Acad. Sci. U.S.A. · 2009 · 106 · 1272910.1073/pnas.0902621106 ↗
4. Diao J. · Nat. Protoc. · 2012 · 7 · 92110.1038/nprot.2012.020 ↗
5. Czolkos I. · Soft Matter · 2011 · 7 · 456210.1039/c0sm01212b ↗
6. Nollert P. · Biophys. J. · 1995 · 69 · 144710.1016/S0006-3495(95)80014-7 ↗
7. Cremer P. S. · J. Phys. Chem. B · 1999 · 103 · 255410.1021/jp983996x ↗
8. Richter R. P. · Langmuir · 2006 · 22 · 349710.1021/la052687c ↗
9. Keller C. A. · Biophys. J. · 1998 · 75 · 139710.1016/S0006-3495(98)74057-3 ↗
10. Reviakine I. · Langmuir · 2000 · 16 · 180610.1021/la9903043 ↗
11. Seifert U. · Phys. Rev. A · 1990 · 42 · 476810.1103/PhysRevA.42.4768 ↗
12. Lipowsky R. · Mol. Cryst. Liq. Cryst. · 1991 · 202 · 1710.1080/00268949108035656 ↗
13. Seifert U. · Adv. Phys. · 1997 · 46 · 1310.1080/00018739700101488 ↗
14. Keller C. A. · Phys. Rev. Lett. · 2000 · 84 · 544310.1103/PhysRevLett.84.5443 ↗
15. Richter R. · Biophys. J. · 2003 · 85 · 303510.1016/S0006-3495(03)74722-5 ↗
16. Richter R. P. · Biophys. J. · 2005 · 88 · 342210.1529/biophysj.104.053728 ↗
17. Johnson J. M. · Biophys. J. · 2002 · 83 · 337110.1016/S0006-3495(02)75337-X ↗
18. Mashaghi A. · Anal. Chem. · 2008 · 80 · 366610.1021/ac800027s ↗
19. Edvardsson M. · Anal. Chem. · 2009 · 81 · 34910.1021/ac801523w ↗
20. Benes M. · Langmuir · 2004 · 20 · 1012910.1021/la048811u ↗
21. Reimhult E. · Langmuir · 2003 · 19 · 168110.1021/la0263920 ↗
22. Anderson T. H. · Langmuir · 2009 · 25 · 699710.1021/la900181c ↗
23. Reimhult E. · J. Chem. Phys. · 2002 · 117 · 740110.1063/1.1515320 ↗
24. Reimhult E. · Phys. Rev. E · 2002 · 66 · 05190510.1103/PhysRevE.66.051905 ↗
25. Cho N. J. · Langmuir · 2011 · 27 · 373910.1021/la104348f ↗
26. Hain N. · Langmuir · 2013 · 29 · 228210.1021/la304197m ↗
27. Reimhult E. · Anal. Chem. · 2004 · 76 · 721110.1021/ac0492970 ↗
28. Weirich K. L. · Biophys. J. · 2010 · 98 · 8510.1016/j.bpj.2009.09.050 ↗
29. Reimhult E. · Langmuir · 2006 · 22 · 331310.1021/la0519554 ↗
30. Dimitrievski K. · Colloids Surf., B · 2006 · 47 · 11510.1016/j.colsurfb.2005.12.002 ↗
31. Reviakine I. · J. Chem. Phys. · 2005 · 122 · 20471110.1063/1.1908500 ↗
32. Hamai C. · Biophys. J. · 2006 · 90 · 124110.1529/biophysj.105.069435 ↗
33. Schonherr H. · Langmuir · 2004 · 20 · 1160010.1021/la049302v ↗
34. Lenz P. · Europhys. Lett. · 2006 · 75 · 65910.1209/epl/i2006-10150-5 ↗
35. Lindfors K. · Phys. Rev. Lett. · 2004 · 93 · 03740110.1103/PhysRevLett.93.037401 ↗
36. Kukura P. · Nat. Methods · 2009 · 6 · 92310.1038/nmeth.1395 ↗
37. Ortega-Arroyo J. · Phys. Chem. Chem. Phys. · 2012 · 14 · 1562510.1039/c2cp41013c ↗
38. Kukura P. · J. Phys. Chem. Lett. · 2010 · 1 · 332310.1021/jz101426x ↗
39. Ewers H. · Nano Lett. · 2007 · 7 · 226310.1021/nl070766y ↗
40. Mlodzianoski M. J. · Opt. Express · 2009 · 17 · 826410.1364/OE.17.008264 ↗
41. Jacobsen V. · Opt. Express · 2006 · 14 · 40510.1364/OPEX.14.000405 ↗
42. Kukura P. · Nano Lett. · 2009 · 9 · 92610.1021/nl801735y ↗
43. Krishnan M. · Nature · 2010 · 467 · 69210.1038/nature09404 ↗
44. Betzig E. · Science · 2006 · 313 · 164210.1126/science.1127344 ↗
45. Brokmann X. · Chem. Phys. · 2005 · 318 · 9110.1016/j.chemphys.2005.06.032 ↗
46. Parker J. L. · J. Phys. Chem. · 1989 · 93 · 612110.1021/j100353a034 ↗
47. Evans E. · Phys. Rev. Lett. · 1990 · 64 · 209410.1103/PhysRevLett.64.2094 ↗
48. Kuo C. K. · J. Am. Chem. Soc. · 2011 · 133 · 466410.1021/ja1099193 ↗
49. Kalb E. · Biochim. Biophys. Acta · 1992 · 1103 · 30710.1016/0005-2736(92)90101-Q ↗
50. Considine P. S. · J. Opt. Soc. Am. · 1966 · 56 · 100110.1364/JOSA.56.001001 ↗